Longitudinal evaluation of glucose tolerance and insulin secretion in non-diabetic children and adolescents with cystic fibrosis: results of a two-year follow-up

Acta Paediatr. 1993 Mar;82(3):249-53. doi: 10.1111/j.1651-2227.1993.tb12653.x.

Abstract

Thirty-two patients with cystic fibrosis and repeatedly normal fasting blood glucose underwent oral glucose tests and islet-cell antibody assessments on two occasions approximately two years apart. Fourteen patients underwent two iv glucose tolerance tests also. Although in the group as a whole mean glucose areas in response to the oral test remained substantially unmodified over the two-year period, the prevalence of glucose tolerance abnormalities increased from 37.5 to 50%. Insulin output in response to both oral and iv tolerance tests decreased over time. Worsening of insulin secretion and/or of glucose tolerance was never accompanied by deteriorating clinical status. Islet-cell antibodies were detected in no patients, even in those who developed a diabetic glucose tolerance. These results support, on a longitudinal basis, the view of a progressive impairment of B-cell function in cystic fibrosis, which may precede the onset of metabolic abnormalities and is not triggered by autoimmunity.

MeSH terms

  • Adolescent
  • Adult
  • Autoantibodies / blood
  • Blood Glucose / analysis*
  • Child
  • Cystic Fibrosis / blood*
  • Follow-Up Studies
  • Glucose Tolerance Test / methods
  • Humans
  • Insulin / metabolism*
  • Insulin Secretion
  • Islets of Langerhans / immunology
  • Longitudinal Studies
  • Male
  • Prospective Studies

Substances

  • Autoantibodies
  • Blood Glucose
  • Insulin